A yolk-shell structured metal-organic framework with encapsulated iron-porphyrin and its derived bimetallic nitrogen-doped porous carbon for an efficient oxygen reduction reaction
A yolk-shell structured metal-organic framework (MOF) with encapsulated 5,10,15,20-tetraphenylporphyrinatoiron (FeTPP) in a zeolitic imidazolate framework (ZIF)-L-ZIF-8 is reported. ZIF-L with leaf-like morphology is used as a core, and FeTPP molecules will induce the partial decomposition of ZIF-L....
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-05, Vol.8 (19), p.9536-9544 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A yolk-shell structured metal-organic framework (MOF) with encapsulated 5,10,15,20-tetraphenylporphyrinatoiron (FeTPP) in a zeolitic imidazolate framework (ZIF)-L-ZIF-8 is reported. ZIF-L with leaf-like morphology is used as a core, and FeTPP molecules will induce the partial decomposition of ZIF-L. The ZIF-8 shell is formed and encapsulates FeTPP in the yolk-shell structure by adding Zn ions and 2-methylimidazole (Hmim). After pyrolysis, FeCo bimetallic nitrogen doped porous carbon (FeCo-C/N) exhibits ORR performance comparable to commercial Pt/C (20 wt%), with a significant decrease in cost. Density functional theory (DFT) calculations demonstrate that the Fe site in FeCo-C/N contributes to the improved ORR performance by reducing the formation energy of *OOH formation. Thus, a Zn-air battery with FeCo-C/N as an electrocatalyst exhibits significantly improved performance (a high peak power density of 397.25 mW cm
−2
, and good rechargeable stability). The synthesis strategy presented in this work provides new opportunities for designing yolk-shell structured 2D MOFs for applications in energy conversion and storage.
A yolk-shell structured metal-organic framework (MOF) with encapsulated 5,10,15,20-tetraphenylporphyrinatoiron (FeTPP) in a zeolitic imidazolate framework (ZIF)-L-ZIF-8 is reported. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta00962h |